A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5484064



Internal ID261486
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:19143076..19156984hg38UCSC Ensembl
chr9:19143074..19156982hg19UCSC Ensembl
Cytoband9p22.1
Allele length
AssemblyAllele length
hg3813909
hg1913909
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17020802
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5484064
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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